|Publication number||US4257934 A|
|Application number||US 06/092,246|
|Publication date||Mar 24, 1981|
|Filing date||Nov 7, 1979|
|Priority date||Nov 7, 1979|
|Publication number||06092246, 092246, US 4257934 A, US 4257934A, US-A-4257934, US4257934 A, US4257934A|
|Inventors||Joseph F. O'Mahoney, Jr.|
|Original Assignee||The Goodyear Tire & Rubber Company|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (5), Referenced by (9), Classifications (17)|
|External Links: USPTO, USPTO Assignment, Espacenet|
This invention relates to compounded EPDM/SBR/SB resin mixtures that exhibit in cured state greatly enhanced modulus values, wherein EPDM designates an ethylenepropylene dimer rubber, SBR designates a rubbery copolymer of styrene-butadiene and SB resin designates a nonrubbery copolymer of styrene-butadiene having at least 80 percent styrene.
Generally the vulcanizates of EPDM/SBR/SB resin blends have a modulus of 10,000 to 17,000 pounds per square inch. This is a decided disadvantage as these vulcanizates are finding commercial use as stiff flexible components in automotive body parts and as paints for flexible parts.
It was discovered that the modulus of the vulcanizates of EPDM/SBR/SB resin blends could be increased by at least 10 percent, and in many cases by 100 percent or more, by including a small amount of a nonreinforcing resin of the tackifier class in the blend. This is indeed unexpected and unobvious as generally these nonreinforcing aromatic resins, such as the so-called tackifier resins, act as diluents and reduce the physical properties of the resulting vulcanizates.
Representative classes of the nonreinforcing resins of the tackifier class useful in this invention are the coal tar resins, petroleum resins, polyterpene resins and the aromatic resins. Some specific examples of these resins are the coumarone-indene resins, polystyrenated aromatic resins, polynuclear aromatic resins, alkyl aromatic hydrocarbon resins, phenolic modified terpene resins, polymerized rosin esters, styrene acrylic comonomer resins, α-methylstyrene resins, solvent pine resin (available under the trademark Vinsol), phenolic modified terate resins, and diphenyl and polyphenyl aromatic hydrocarbons. These resins normally have melting points of about 100° C. to 165° C. The higher the melting point the more pronounced the enhancement of modulus. Usually 1 to 20 parts of nonreinforcing aromatic resin per 100 parts of rubber (phr), viz. the three component blend, can be used with the preferred range being 3 to 6 phr.
The nature of this invention can be more fully appreciated from the following representative examples wherein all parts and percentages are by weight unless otherwise indicated.
For convenience of illustration a master recipe is set forth below to which the nonreinforcing aromatic resins are added to give the compounded rubbers of this invention but it should be appreciated that in practice the rubber compounder might prefer to add the ingredients of the recipe in a different manner or order during the compounding, for instance on the mill.
The master recipe has the following composition:
______________________________________Ingredient Parts______________________________________Styrene-butadiene rubber 60.00Butadiene-styrene resin, 17.5% butadiene 25.00EPDM rubber 40.00Carbon black FEF 80.00Zinc oxide 5.00Stearic acid 2.00Antioxidant, phenolic type 1.00Accelerator, sulfenamide type 1.75Scorch inhibitor (optional ingredient) 0.15 217.90______________________________________
This master recipe yielded a vulcanizate having modulus values of less than 17,000 but when various nonreinforcing tackifying resins were added the modulus was greatly enhanced.
When 1 part of polynuclear aromatic resin of 100° C. melting point, 4 parts coumarone-indene resin of 100° C. melting point was compounded on the mill into 217.9 parts of the above composition of the recipe the resulting vulcanizate, 12 to 15 minutes at 165°, had modulus values in excess of 23,000.
When the master recipe was varied to increase the butadiene-styrene resin content to 30 parts instead of 25 and the carbon black content was raised to 85 parts and the tackifying resins level raised to 20 parts of coumarone-indene resin of 126° C. melting point the flexural modulus values of the vulcanizate were raised to 38,000 pounds per square inch. When the 126° C. melting point coumarone-indene was replaced in the above modified recipe with the corresponding 155° C. melting point coumarone-indene resin the flexural modulus values of its vulcanizate was 46,000. Likewise when the low melting coumarone-indene resin was replaced by either of the following tackifying resins: alkyl aromatic hydrocarbon resin 110/120° C. melting point (available under the trade name Piccoumaron 110 and 120), phenolic modified terpene resin 125° C. melting point (available under the trade name Piccofyn D125), styrene-acrylic copolymer resin 146° C. melting point (available under the trade name Piccotoner), and alpha methyl styrene resin 120° C. melting point (available under the trade name Kristoflex), the vulcanizates had flexural modulus approaching 30,000 and up to about 45,000.
When pine stump wood resin (available under the trademark Vinsol) 120° melting point is used the paint made from the compound blend tends to be staining, thus higher pigment loadings may be desirable, but the flexural modulus of the vulcanizate is in the 40,000 range or higher.
These experiments illustrate the magnitude of the flexural modulus obtainable in accordance with this invention.
While certain representative embodiments and details have been shown for the purpose of illustrating the invention it will be apparent to those skilled in this art that various changes and modifications may be made therein without departing from the spirit or scope of the invention.
|Cited Patent||Filing date||Publication date||Applicant||Title|
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|US3634352 *||Aug 29, 1969||Jan 11, 1972||Us Agriculture||Synthetic rubber compositions tackified by modified pine gum|
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|Citing Patent||Filing date||Publication date||Applicant||Title|
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|WO2010102044A2||Mar 3, 2010||Sep 10, 2010||Gidi Shani||Volume adjusted preservation containment system|
|U.S. Classification||524/271, 525/206, 525/133, 525/211, 525/227, 525/185|
|International Classification||C08L9/06, C08L25/10, C08L23/16|
|Cooperative Classification||C08L45/02, C08L93/00, C08L25/10, C08L9/06, C08L23/16|
|European Classification||C08L23/16, C08L9/06, C08L25/10|